Kah&Mac lab: Difference between revisions
No edit summary |
|||
Line 12: | Line 12: | ||
mission of the National Institutes of Health (NIH; Brook, 2012; Emerson et al., 2010; Metan et al., 2006). Currently, there are critical knowledge gaps with respect to how ''S. maltophilia'' avoids clearance by humoral and cellular components of the immune system and how biofilm communities are established ''in vivo''. We are using a variety of forward genetic screens to identify bacterial factors involved in colonization of biotic and abiotic surfaces, host cell toxicity, and immune evasion.<br> | mission of the National Institutes of Health (NIH; Brook, 2012; Emerson et al., 2010; Metan et al., 2006). Currently, there are critical knowledge gaps with respect to how ''S. maltophilia'' avoids clearance by humoral and cellular components of the immune system and how biofilm communities are established ''in vivo''. We are using a variety of forward genetic screens to identify bacterial factors involved in colonization of biotic and abiotic surfaces, host cell toxicity, and immune evasion.<br> | ||
====Virulence Priming of Opportunistic Pathogens==== | |||
====Invertebrate Assays of Bacterial Virulence==== | |||
Revision as of 22:05, 29 April 2014
Welcome to the Fisher Lab WikiWe combine genetic, biochemical, molecular, and genomic approaches with a variety of high-throughput host systems to address questions of fundamental concern to human health and agriculture. Colonization and Innate Immune Evasion by the Emerging Opportunistic Pathogen Stenotrophomonas maltophiliaS. maltophilia is an emerging, multi-drug-resistant (MDR), opportunistic pathogen that frequently colonizes ventilator tubes and indwelling medical devices where it forms biofilms. Initial colonization can lead to severe, life-threatening infection and recent studies show that both incidence and prevalence are increasing, especially in immunocompromised, cystic fibrosis, chronic obstructive pulmonary disease (COPD), and cancer patients—demographic groups key to the research
mission of the National Institutes of Health (NIH; Brook, 2012; Emerson et al., 2010; Metan et al., 2006). Currently, there are critical knowledge gaps with respect to how S. maltophilia avoids clearance by humoral and cellular components of the immune system and how biofilm communities are established in vivo. We are using a variety of forward genetic screens to identify bacterial factors involved in colonization of biotic and abiotic surfaces, host cell toxicity, and immune evasion. Virulence Priming of Opportunistic PathogensInvertebrate Assays of Bacterial VirulenceJoin UsWe are always interested in motivated students, please submit inquiries via the contact tab. |